nsv6624316
- Organism: Homo sapiens
- Study:nstd224 (Zarrei et al. 2023)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:15,104
- Publication(s):Zarrei et al. 2023
Source: NCBI
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 399 SVs from 60 studies. See in: genome view
Overlapping variant regions from other studies: 395 SVs from 60 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv6624316 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000017.11 | Chr17 | 79,379,540 | 79,394,643 |
| nsv6624316 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000017.10 | Chr17 | 77,375,622 | 77,390,725 |
Variant Call Information
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18307490 | Remapped | Perfect | NC_000017.11:g.(?_ 79379540)_(7939464 3_?)dup | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 79,379,540 | 79,394,643 |
| nssv18320505 | Remapped | Perfect | NC_000017.11:g.(?_ 79379540)_(7939464 3_?)dup | GRCh38.p12 | First Pass | NC_000017.11 | Chr17 | 79,379,540 | 79,394,643 |
| nssv18307490 | Submitted genomic | NC_000017.10:g.(?_ 77375622)_(7739072 5_?)dup | GRCh37 (hg19) | NC_000017.10 | Chr17 | 77,375,622 | 77,390,725 | ||
| nssv18320505 | Submitted genomic | NC_000017.10:g.(?_ 77375622)_(7739072 5_?)dup | GRCh37 (hg19) | NC_000017.10 | Chr17 | 77,375,622 | 77,390,725 |